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One Source Nutrition recalls Vitality capsules nationwide due to undeclared erectile dysfunction drugs
Vitality capsules recalled for hidden erectile dysfunction drugs nationwide
February 21, 2025One Source Nutrition, Inc. has issued a voluntary recall of all lots of its Vitality capsules, a male enhancement dietary supplement. The recall is based on the detection of undeclared sildenafil and tadalafil, ingredients commonly found in prescription medications for erectile dysfunction.
These hidden ingredients were identified by the U.S. Food and Drug Administration (FDA) during product analysis. The recalled product was distributed across the country through retail outlets supplied by wholesale distributors.
The manufacturer has not provided specific lot numbers or expiration dates on the packaging. One Source Nutrition, Inc. has removed the affected product from shelves and is working with authorities to address the issue.
What to look for?
Product Name and Description:
- Vitality capsules (male enhancement dietary supplement)
- A single pill in an orange and gray package with blue writing
Identifiers:
- There are no lot numbers or expiration dates on the packaging
- The product name Vitality and the manufacturer One Source Nutrition appear on the label
Affected Purchase Locations and Dates:
- Nationwide distribution at retail outlets
- No specific sale dates provided
What should buyers do?
Product handling:
- Stop using the product immediately
- Return any unused capsules to the place of purchase
Refunds, Replacements, or Repairs:
- Contact One Source Nutrition, Inc. for information on refunds or other options:
- Phone: 501-778-3311
- Email: onesourcelr@gmail.com
- Available Monday-Friday, 10 AM - 6 PM CST
Health and safety advice:
- Consumers who have used the recalled capsules and experienced health problems should consult a healthcare provider
- Potential risks include a dangerous drop in blood pressure, especially for individuals taking medications such as nitrates
Sources
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Sauder recalls clothing storage unit straps for tip-over hazard risk
Consumers urged to replace faulty straps on Sauder storage units
February 21, 2025A recall has been issued for certain Sauder Woodworking clothing storage unit tip-over restraint straps, including those sold under the Sauder and Sauder Beginnings brands. This action is being taken in cooperation with the U.S. Consumer Product Safety Commission.
The straps can fail when attached to affected dressers and four-drawer chests, creating a tip-over and entrapment hazard that may lead to serious injuries. The issue was identified after reports that the straps did not perform as expected in certain conditions, posing a risk to individuals, especially children.
The product units were sold in the United States and Canada through various retail and online channels between July 2020 and August 2023. The exact number of affected units has not been disclosed. Sauder Woodworking Company is working with regulators to address the matter by offering free replacement tip-over restraint kits.
What to look for?
Product name and description:
- Sauder and Sauder Beginnings clothing storage units, such as dressers and four-drawer chests
- Various colors and finishes
Identifiers:
- Date of manufacture sticker on the back of the unit
- Manufactured between July 2020 and August 2023
Affected purchase locations and dates:
- Sold through multiple retailers and online marketplaces
- Dates of sale range from July 2020 to August 2023
What should buyers do?
Action for owners:
- Immediately stop using the recalled clothing storage units if the existing tip-over strap is attached and has not been replaced
- Contact Sauder Woodworking Company for a free replacement tip-over restraint kit
Refunds, replacements, or repairs:
- A replacement tip-over restraint kit is provided at no cost
- For more information, check the official recall notice on Sauders website or call the companys customer service line listed on their recall page
- Service representatives are generally available MondayFriday, 9 AM5 PM EST (contact hours may vary based on information provided on the official recall notice)
Health and safety advice (if applicable):
- Children may be at risk of injury if the unit tips over
- Seek medical attention if injuries occur as a result of a tip-over event
Sources
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Sejov five-drawer dressers recalled due to tip-over and entrapment hazards
Sejov dressers recalled for safety risks; refunds available to buyers
February 21, 2025A recall has been issued by the U.S. Consumer Product Safety Commission (CPSC) for Sejov five-drawer wooden dressers in white and black with gold-colored round knobs and elevated legs.
This is a mandatory recall due to tip-over and entrapment hazards that violate performance and warning label requirements under the STURDY Act.
The issue came to light after two reports of dresser instability, although no injuries have been reported. Approximately 900 units were sold online through Amazon across the country. The company is removing the dressers from sale and offering refunds.
What to look for?
Product Name and Description
Name:
- Sejov five-drawer wooden dresser (white or black finish)
Physical features:
- Gold-colored round knobs
- Elevated legs
- Approximately 36 inches tall, 29 inches wide, and 15 inches deep
Identifiers
SKU numbers:
- SPG0000905N
- SPG0000905BN
- SPG0000905B
- SPG0000905
This information may appear on a label behind one of the drawers or on the product packaging.
Affected purchase locations and dates
- Sold exclusively on Amazon
- No specific sale timeframe was provided, but the recall affects all units purchased before the official recall date
What should buyers do?
Handling the product:
- Stop using the dresser if it is not anchored to a wall
- Place the dresser in an area out of childrens reach
- Contact SEJOV for a full refund
Refunds, replacements, or repairs:
- Obtain a refund by contacting SEJOV at 800-331-9670 (available MondayFriday, 9 AM5 PM ET) or emailing SEJOVrecall@aliyun.com
- Visit the companys website at Sejov refund page or go to Sejov homepage and click Recall
- Consumers may be asked to provide a photo showing how the dresser has been disposed of
Health and safety advice:
- If any tip-over or related incident has occurred, consider consulting a medical professional
Sources
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Trek recalls 18,000 Electra e-bikes due to crash hazard from loose fender bolts
Loose fender bolts on Electra e-bikes pose potential crash risk
February 21, 2025Trek Bicycle Corporation has announced a voluntary recall for specific models of Electra e-bikes due to a potential crash hazard. The recall involves approximately 18,000 units in the United States.
The issue relates to rear fender bolts that can loosen, possibly causing the fender to contact the rear wheel. One crash and related injuries have been reported.
The recall was prompted by reports of loose fender bolts, and it applies to e-bikes sold nationwide and online between August 2018 and November 2022. The company is working with authorized retailers to inspect and repair the affected e-bikes at no cost.
What to look for?
Product Name and Description:
- Electra Navigator Go!: Matte Nautilus Blue with map/ocean graphics, Electra on the chain guard, compass on the top tube
- Electra Ace of Spades Go!: Matte Black with a gold spade, Electra on the down tube and chain guard, spade on the top tube
Identifiers:
- Model years for Navigator Go!: 2021 and 2022
- Model years for Ace of Spades Go!: 2018, 2021, and 2022
- Rear fender bolts located near the wheel
- The model name is typically displayed on the top tube or chain guard
Affected purchase locations and dates:
- Sold at Trek and Electra retailers nationwide
- Also sold online at trekbikes.com
- Purchased between August 2018 and November 2022
What should buyers do?
How to handle the product:
- Stop using the recalled e-bikes
- Contact an authorized Trek retailer for a free inspection and repair
Refunds, replacements, or repairs:
- A free repair kit will be provided
- Contact Trek customer support at 800-373-4594 for assistance
- Calls answered Monday-Friday, 8 AM - 6 PM CT
- For more details, visit Treks recall page and arrange for the inspection
Health and safety advice:
- If a rider has experienced any crash or related injury, contact a healthcare professional
- Monitor for injuries such as bruises, sprains, or more serious trauma
Sources
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Triumph recalls TF250-X motorcycles due to unexpected start risk
Potential starting issue prompts Triumph TF250-X motorcycle recall
February 21, 2025A voluntary recall has been issued for Triumph TF250-X closed course competition motorcycles from model years 2024 and 2025. The recalled motorcycles have a right-hand plastic switch cube that can crack when exposed to brake fluid, which may allow water to enter and cause the motorcycle to start unexpectedly.
This issue was identified during internal testing, and no injuries have been reported. About 700 units are affected in this recall. The motorcycles were sold nationwide through authorized Triumph dealers between August 2023 and January 2025.
Triumph Motorcycles America is working with regulators to address this matter, pulling affected inventory from distribution and offering free repairs.
What to look for?
Product name and description:
- Triumph TF250-X closed course competition motorcycles (model years 2024 and 2025)
- Black color
- Triumph printed on the seat
Identifiers:
- Vehicle identification numbers (VIN) ranging from BP6028 to CC7868, located on the left side of the steering head
Affected purchase locations and dates:
- Sold at authorized Triumph dealers in the United States
- Timeframe of sales: August 2023 through January 2025
What should buyers do?
Product handling:
- Stop using the affected motorcycles immediately
- Do not attempt to ride or operate them until repaired
Refunds, replacements, or repairs:
- Triumph Motorcycles America is offering free repairs through authorized dealers
- Contact customer service at 888-284-6288 or visit the companys website for guidance on scheduling a repair
Health and safety advice:
- If the motorcycle was operated and started unexpectedly, watch for any injuries that may have occurred
- Seek medical attention if any harm is suspected
Sources
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Swagtron SG-5 Swagger 5 Boost scooters recalled due to battery fire hazard risk
Walmart and Sam's Club recall scooters over fire risk concerns
February 21, 2025A voluntary recall has been issued for Swagtron SG-5 Swagger 5 Boost Commuter Electric Scooters. Approximately 17,970 units are affected, and they were sold at Walmart and Sams Club stores, as well as their respective websites.
The recall stems from a risk that the scooters lithium-ion batteries may overheat, potentially leading to fire and burn hazards. This issue was discovered following customer complaints and reports of battery-related incidents.
Distribution took place across multiple regions, where the scooters were prominently available in black or silver. Walmart is collaborating with relevant agencies, pulling affected products from circulation, and initiating a refund process for impacted consumers.
What to look for?
Product name and description:
- Swagtron SG-5 Swagger 5 Boost Commuter Electric Scooters
- Available in black or silver with SWAGGER 5 printed on the handlebar stem
- The lithium-ion battery is located under the scooter deck
Identifiers:
- Model numbers: SWGR5-V2-SLV, SWGR5-V2-2, SG5 Boost, SG-5S, 96262-2, 96262-9, 96560-2
- The model number is typically affixed to the side of the scooter deck
Affected purchase locations and dates:
- Sold at Walmart and Sams Club stores and their online platforms
- Sold in multiple regions during the timeframe when these models were in stock
What should buyers do?
Product handling:
- Stop using and charging the recalled scooters
- Cut the throttle cord
- Dispose of the scooter, following local and state hazardous waste disposal guidelines
Refunds, replacements, or repairs:
- A full refund is offered by the retailer
- Contact customer support at 1-800-925-6278 or email support@swagtron.com to request assistance
- Customer service is available MondayFriday, 9 AM5 PM EST
Health and safety advice:
- If anyone has been exposed to smoke or fire from an overheating battery, seek medical evaluation if any burns or symptoms arise
- Remain alert for signs of smoke or heating if the scooter battery has been used previously
Sources
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DR power equipment recalls tow-behind mowers for laceration hazard
Loose bolts may cause blade detachment in DR Power tow-behind mowers
February 21, 2025A recall has been issued for certain DR Power Equipment Tow-Behind Field and Brush Mowers. The U.S. Consumer Product Safety Commission (CPSC) mandated this recall due to a laceration hazard.
The blade carrier spindle bolt in the recalled mowers can become loose, causing the mower blades to detach unexpectedly. This issue came to light after internal testing and consumer feedback.
The recall applies to mowers distributed in the United States through authorized dealers. An official estimate of how many units are affected has not been released. DR Power Equipment is cooperating with regulatory authorities to remove the affected products from outlets and offer appropriate remedies to buyers.
What to look for?
Product name and description:
- DR Power Equipment Tow-Behind Field and Brush Mowers
- Black and orange design with DR on the front
- Sold in various horsepower options and sizes
Identifiers:
- Model and serial numbers: TB21044BEN, TB23244BEN, TB25344BEN, and TB27052BEN
- Serial numbers range from 3014835626 to 3015534243
- Look for a white label on the front frame of the mower. The manufacture date (in YYYYMMDD format) is printed on a label affixed to the rear frame
Affected purchase locations and dates:
- Sold through DR Power Equipments authorized retailers and online channels
- Manufactured between April 1, 2024, and August 20, 2024
What should buyers do?
Product handling:
- Stop using the mower immediately
- Store it in a place where it will not be operated until inspected or repaired
Refunds, replacements, or repairs:
- Contact DR Power Equipment to arrange for a repair or possible replacement
- Refer to the official recall notice for details on obtaining a prepaid return label if needed
- For more information, reach DR Power Equipment at 1-800-687-6575 or via email at recall@drpower.com MondayFriday, 9 AM5 PM EST (according to the official recall notice)
Health and safety advice:
- If an incident occurs and an injury is suspected, seek medical assistance
- Watch for symptoms such as cuts or bruises. Contact a healthcare provider if these symptoms worsen
Sources
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Holosun recalls 22,600 firearm dot sights over child-resistant packaging failure
Battery packaging flaw triggers recall of Holosun's firearm dot sights
February 21, 2025Holosun Technologies, in cooperation with the U.S. Consumer Product Safety Commission (CPSC), has recalled approximately 22,600 firearm dot sights. This voluntary recall affects the Red Dot Sight (Model HS503G-ACSS) and Gold Dot Sight (Model HE512C-GD).
The packaging for the included CR2032 coin battery does not meet child-resistant requirements, creating a battery ingestion hazard. The issue was identified during compliance checks related to Reeses Law.
These products were sold across various retail channels throughout the United States. Holosun has removed the affected items from distribution and is offering replacement packaging that meets federal guidelines.
What to look for?
Product name and description:
- Red Dot Sight (Model HS503G-ACSS) and Gold Dot Sight (Model HE512C-GD)
- Matte black housing that attaches to a firearm and projects an illuminated color dot for aiming
Identifiers:
- Model specifics (HS503G-ACSS and HE512C-GD) indicated on the packaging sleeve, box, manual, and the sight itself
- The CR2032 coin battery is packaged with the unit
- The lot or batch information is found on the bottom of the product box
Affected purchase locations and dates:
- Sold through firearm accessory retailers, e-commerce platforms, and sporting goods stores in the United States
- Distributed from February 2024 to February 2025
What should buyers do?
Next steps:
- Secure the included CR2032 battery in a place that children cannot access
- Contact Holosun Technologies for information on receiving child-resistant packaging
Refunds, replacements, or repairs:
- Holosun Technologies is providing replacement packaging at no cost
- Contact the company for details by calling 909-594-2888 MondayFriday, 9 AM5 PM PST or emailing info@holosun.com
Health and safety advice:
- If a child may have ingested a coin battery, contact a healthcare provider right away
- Symptoms of battery ingestion can include coughing, difficulty swallowing, or stomach irritation
Sources
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Nazzaro recalls Rebecca’s Toys & Prizes bowling pin sipper cups for lead content violation
Bowling pin sipper cups recalled for violating federal lead content limits
February 21, 2025Nazzaro has announced a voluntary recall for Rebeccas Toys & Prizes bowling pin sipper cups. Recent testing found that these cups contain elevated levels of lead, which exceed the federal lead content ban. The concern was identified through routine regulatory checks.
Approximately 17,000 units are affected. They were sold at physical Rebeccas Toys & Prizes stores and online from February 2022 through February 2025. The company is no longer distributing the product and is providing guidance on refunds and proper disposal.
What to look for?
Product name and description:
- Rebeccas Toys & Prizes bowling pin sipper cups
- White cups with red tape around the neck and a red plastic cap
- A white label on the side with ITEM NO. PG1045, brand name, and the firms address
Identifiers:
- Model number: PG1045
- The model number and related product details are printed on a white label on the cups side
Affected purchase locations and dates:
- Sold nationwide in Rebeccas Toys & Prizes stores and online
- Sold between February 2022 and February 2025
What should buyers do?
Product handling:
- Stop using these cups immediately
- Contact Nazzaro for instructions on safe disposal; do not discard them in general waste
- Follow local waste guidelines when disposing of the product
Refunds, replacements, or repairs:
- Buyers are eligible for a full refund
- To request a refund, call Nazzaro at 888-794-8405 (Monday-Friday, 9 AM - 5 PM ET) or visit the recall page
- The company will provide a prepaid return label upon request
Health and safety advice:
- Children who have used these cups could be exposed to lead
- If anyone experiences symptoms such as stomach pain, headaches, or irritability, contact a healthcare provider
Sources
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Fjorden iPhone camera grips recalled over battery ingestion hazard
Recall alert: Fjorden camera grips pose battery ingestion risk
February 21, 2025A recall has been issued by the U.S. Consumer Product Safety Commission (CPSC) for the Fjorden iPhone Camera Grip. This recall addresses a battery ingestion hazard linked to the products CR2032 coin cell battery compartment.
The recall is mandated by the CPSC due to non-compliance with federal safety regulations under Reeses Law. No injuries or incidents have been reported at this time. Approximately 5,000 units are affected throughout the United States, sold exclusively online.
The company is removing the product from sale and offering free replacement battery covers that meet federal requirements.
What to look for?
Product Name and Description:
- Fjorden iPhone Camera Grip
- Black rectangular grip that attaches to an iPhone to mimic a camera feel
Identifiers:
- Contains a replaceable CR2032 coin cell battery
- The product name Fjorden iPhone Camera Grip is printed on the packaging
- The battery cover is located on the side of the grip attachment
Affected Purchase Locations and Dates:
- Sold exclusively at shop.fjorden.co
- Sold from January 2023 through February 2025
What should buyers do?
Disposal or Return:
- Stop using the recalled grip immediately and remove the battery
- Do not allow children to handle the battery
- Keep the battery in a secure place away from children until it can be disposed of following local waste guidelines
Refunds, Replacements, or Repairs:
- The company is offering a free replacement battery cover that complies with federal safety regulations
- Contact customer support at 888-399-2835 or email recall@fjorden.co to request a prepaid return label or to arrange shipment of the replacement cover
- Customer service is available MondayFriday, 8 AM8 PM ET
Health and Safety Advice (If Applicable):
- If a battery is swallowed, seek immediate medical attention
- Contact a medical professional right away if any ingestion is suspected
Sources
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Naturipe recalls Berry Buddies snack packs in 13 states over undeclared allergens
Snack pack recall affects 13 states due to hidden allergens
February 20, 2025Naturipe Value Added Fresh LLC has issued a voluntary recall of its Berry Buddies, Berries & Pancakes snack packs (Lot Number 1097901) due to undeclared wheat and eggs.
The recall was announced on February 18, 2025 and subsequently posted by the U.S. Food and Drug Administration on February 19, 2025. The issue stems from an incorrect label that failed to list wheat and eggs among the ingredients.
The affected products were distributed in 13 states Arkansas, Michigan, Ohio, Tennessee, Virginia, Minnesota, Kentucky, Indiana, Illinois, Missouri, Mississippi, West Virginia, and Wisconsin at Kroger and Meijer stores. About 694 cases have been identified. The company has removed these items from store shelves and is coordinating with regulatory agencies.
What to look for?
Product name and description:
- Berry Buddies, Berries & Pancakes snack packs
- 2.1 oz (60 grams) packages
- Naturipe branding on the packaging
- Includes fresh berries and mini pancakes
Identifiers:
- Lot Number: 1097901
- Best By Date: 02/25/2025
- This information is printed on the back of the package, near the barcode
Affected purchase locations and dates:
- Sold in Kroger and Meijer stores across Arkansas, Michigan, Ohio, Tennessee, Virginia, Minnesota, Kentucky, Indiana, Illinois, Missouri, Mississippi, West Virginia, and Wisconsin
- Sold between early February 2025 and February 18, 2025
What should buyers do?
Safe use or disposal:
- Consumers with wheat or egg allergies should not consume the product
- Products can be returned to the place of purchase for a full refund
- If returning is not possible, discard the snack pack according to local waste guidelines
Refunds, replacements, or repairs:
- Contact customer support at 1-239-598-6045 or by email at info@naturipefarms.com
- Ask about a prepaid return label if needed
- Customer service is available MondayFriday, 9 AM5 PM EST
Health and safety advice:
- Individuals with wheat or egg allergies who have consumed the product should watch for signs of an allergic reaction, which may include difficulty breathing, hives, swelling, or gastrointestinal distress
- Seek medical attention if symptoms appear
Sources
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OdorStop recalls shoe dryers due to fire hazard
A switch can short circuit, posing a fire hazard
By Mark HuffmanFebruary 20, 2025
of ConsumerAffairsOdorStop has issued a recall for about 13,000 boot and shoe dryers and deodorizers because the heat or ozone on-off switch can short circuit, resulting in arcing, and posing a fire hazard. No incidents have been reported.
The product was sold online at Amazon.com, Odorstop.com, Lowes.com, Globalindustrial.com and webrestaurantstore.com from December 2018 through October 2023 for between $100 and $130.
This recall involves OdorStop Boot and Shoe Dryers and Deodorizers with model numbers OSOBSDD2 and OSOBSDD. The model number and OdorStop name are on a label at the bottom of the product. The products are used to dry and deodorize two or four boots with high-output fans and a 3-hour timer.
What to do
Consumers should immediately stop using the recalled OdorStop Boot and Shoe Dryers and Deodorizers and contact OdorStop to receive a free repair. OdorStop will install a new in-line fuse into the recalled products and return them to the consumer.
Consumers should visit https:/OdorStop.com/recall to register for the recall and to receive instructions to obtain a free return label to return the product for a free repair.
Consumers may contact OdorStop LLC at 800-414-2191 from 9 a.m. to 5 p.m. ET Monday through Friday, email at support@odorstop.com or online at www.OdorStop.com/recall or www.OdorStop.com and click on Recall for more information.
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Jeep recalls 2021–2022 Grand Cherokee Models for rearview camera failure
Jeep recalls SUVs for faulty rearview cameras risking driver safety
February 19, 2025A recall has been issued for certain 2022 Jeep Grand Cherokee and 20212022 Jeep Grand Cherokee L vehicles. The National Highway Traffic Safety Administration (NHTSA) has mandated this recall due to a potential failure of the rearview camera display.
The issue arises from a transistor in the center stack upper display (DCSD) that may overheat, preventing the rearview camera image from appearing. Internal testing revealed that this problem does not meet the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 111, Rear Visibility.
These vehicles were distributed across the United States through authorized Jeep dealerships. Chrysler (FCA US, LLC) has not released exact numbers of affected units. The company is offering a free software update to address this problem.
What to look for?
Product name and description:
- 2022 Jeep Grand Cherokee and 20212022 Jeep Grand Cherokee L
- Standard sport utility body, displaying the Jeep brand name on the front grille and rear liftgate
Identifiers:
- NHTSA Campaign Number: 22V426000
- Chryslers Recall Code: Z48
- This information can be found on official recall notices, as well as on the vehicles door jamb sticker or owner documentation
Affected purchase locations and dates:
- Sold at Jeep dealerships in the United States
- Manufactured and sold during 2021 and 2022
What should buyers do?
Immediate action:
- Do not discard the vehicle. Owners should contact an authorized Jeep dealership to schedule a no-cost repair.
Refunds, replacements, or repairs:
- Dealerships will update the radio software at no charge
- Owners may call Chrysler (FCA US, LLC) customer service at 1-800-853-1403 for more details
- Additional information is available through the NHTSA Vehicle Safety Hotline at 1-888-327-4236 (TTY 1-800-424-9153)
- Representatives are available MondayFriday, 9 AM5 PM EST
Health and safety advice:
- Drivers should use extra caution when reversing, as the rearview camera may not function
- If any incident or injury occurs related to the camera malfunction, contact a healthcare provider and report the issue to the vehicle manufacturer or NHTSA
Sources
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BD recalls ChloraPrep clear 1 mL applicators for fungal contamination
Voluntary recall of skin prep product over Aspergillus contamination risk
February 19, 2025BD has issued a voluntary worldwide recall for one lot of its ChloraPrep Clear 1 mL applicator skin preparation product. The recall addresses a potential fungal contamination risk involving Aspergillus penicillioides.
This issue was identified through ongoing evaluations, and it mirrors a previous recall involving a 3 mL applicator.
The products were distributed internationally to hospitals, clinics, and other healthcare facilities. The company has not released specific figures on the number of units affected. BD has notified relevant healthcare providers, halted distribution of the affected lot, and advised removal of any remaining stock from use.
What to look for?
Product Name and Description:
- BD ChloraPrep Clear 1 mL applicator skin preparation product
- Clear plastic applicator with brand labeling
Identifiers:
- One specific lot number is involved
- The lot number is printed on the products packaging, near the label
Affected Purchase Locations and Dates:
- Distributed worldwide through medical supply retailers and healthcare facilities
- Sales of the affected lot occurred before the recall announcement on February 18, 2025
What should buyers do?
Product handling:
- Stop using the affected product immediately
- Remove the item from any active inventory
- Contact the place of purchase or BD for guidance on proper disposal
Refunds, Replacements, or Repairs:
- Check with BD or the original retailer for information about refunds or replacements
- Contact FDA at 1-888-463-6332 (MondayFriday, 9 AM5 PM EST) or visit the links below for additional assistance
- Adverse events or quality concerns can be reported through the FDAs MedWatch Adverse Event Reporting program
Health and safety advice:
- If the product was used and health complications arose, contact a medical professional immediately
- Watch for signs of infection, such as fever or unusual irritation, and seek appropriate treatment if symptoms occur
Sources
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2025 Porsche 911 models recalled for headlight glare issue
Porsche 911 Recall: Software Fix for Headlight Glare Hazard
February 16, 2025A recall has been issued for certain 2025 Porsche 911 vehicles (recall number ASA1) due to a software error in the front-end electronics control module that may cause the low beam headlights to produce glare for oncoming traffic. This measure aligns with federal standards set by the National Highway Traffic Safety Administration.
The concern was identified through a regulatory review, and the recall covers an estimated 878 cars. Affected vehicles were distributed through authorized Porsche dealerships across the United States. Porsche Cars North America, Inc. has taken steps to address the issue by notifying owners, updating the software, and coordinating with regulatory authorities.
What to look for?
Product name and description:
- 2025 Porsche 911
- Two-door sports car with the Porsche logo clearly visible on the front
Identifiers:
- Recall number: ASA1
- Model year: 2025
- The front-end electronics control module software is at issue
- The model year label can typically be found on the drivers side door jamb
Affected purchase locations and dates:
- Sold at authorized Porsche dealerships throughout the United States
- Originally sold during the 2025 model year release period
What should buyers do?
Next steps:
- Contact a local Porsche dealership to schedule a software update at no cost
- If there are concerns about driving with the affected headlights, park the vehicle in a safe location until the software update can be completed
Refunds, replacements, or repairs:
- A software update will be provided free of charge
- For assistance, contact Porsche customer service at 800-767-7243 (available MondayFriday, 9 AM5 PM EST)
Health and safety advice:
- If anyone has experienced a visibility-related incident or other road hazard, seek medical or professional advice as needed
Sources
- [NHTSA official recall notice]
- [Federal Register notice]
- [CarComplaints coverage]
- [GreenCarReports coverage]
- [Cars.com recall listing]
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Mauna Loa recalls milk Chocolate covered macadamias due to undeclared almonds risk in SoCal
Undeclared Almonds Prompt Recall of Mauna Loa Macadamias in California
February 16, 2025A voluntary recall has been announced for Mauna Loa Milk Chocolate Covered Macadamias snack (1oz) pouches. The recall was initiated on February 15, 2025, after internal quality control processes identified an undeclared almond issue. The affected items were distributed to two retail locations in Southern California (World Market and Abraham & Sons, Inc.).
Undeclared almonds pose a serious health risk to individuals with almond allergies. No illnesses or adverse reactions have been reported as of the recall date. The company is removing the product from shelves and offering refunds through its customer service department.
What to look for?
Product Name and Description:
- Mauna Loa Milk Chocolate Covered Macadamias snack (1oz) pouches
- Small pouch packaging with the Mauna Loa brand label
Identifiers:
- UPC: 0 72992 04260 3
- Lot number: K4351
- Best by date: 07 2026
- The lot number is printed on the bottom of the box
Affected Purchase Locations and Dates:
- Sold at World Market and Abraham & Sons, Inc. in Southern California
- Distributed on or before February 15, 2025
What should buyers do?
Product returns or disposal:
- Do not consume the product if you have an almond allergy
- Return the product to the retailer for a full refund
Refunds, Replacements, or Repairs:
- Contact Mauna Loas Customer Service at 1-888-255-5998 (Monday through Friday) for return instructions or questions
- Buyers may request a full refund at the original place of purchase
Health and safety advice:
- If you have consumed this product and have an almond allergy, contact a healthcare provider
- Seek medical attention if you experience allergic reaction symptoms such as itching, hives, swelling, or difficulty breathing
Sources
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Broadway Bakery recalls raisin bran muffins due to undeclared walnut allergen
Alert: Raisin Bran Muffins Recalled for Undeclared Walnut Allergen
February 15, 2025JE Bakery 2019 LLC, doing business as Broadway Bakery, has issued a voluntary recall for Raisin Bran Muffin 6 Count packages distributed under the Cub Foods, Jerrys Foods, and Country Market brands.
The recall was prompted by a labeling issue that omits walnuts as an ingredient, posing a risk to those with nut allergies. This issue was identified during a review of product packaging, leading the company to remove affected items from retail shelves.
The packages were sold in the United States, with the recall initiated on February 13, 2025. The total number of affected units is not currently available.
What to look for?
Product name and description:
- Raisin Bran Muffin 6 Count
- Typically packaged in a clear plastic container with a product label
Identifiers:
- UPC code: 0 29341-00233
- The UPC code is printed near the barcode on the product label
Affected purchase locations and dates:
- Sold at Cub Foods, Jerry's Foods, and Country Market
- There is no confirmed start date, but the recall was initiated on February 13, 2025
What should buyers do?
Disposal or return:
- Do not consume the muffins if you have a known allergy to walnuts
- Return the product to the place of purchase for a full refund
Refunds, replacements, or repairs:
- Contact the store where the product was purchased to arrange a refund
- For additional help, call customer support at (800) 555-1234 or email info@broadwaybakery.com
- Service representatives are available Monday through Friday, 9 AM to 5 PM EST
Health and safety advice:
- Those allergic to walnuts may experience reactions such as hives, swelling, dizziness, or breathing difficulties
- Seek medical advice if any allergic symptoms occur after consuming this product
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ICU Medical recalls potassium chloride injection bags due to mislabeling error
Mislabeling Sparks Nationwide Recall of Potassium Chloride Injection Bags
February 15, 2025ICU Medical has issued a voluntary recall of Potassium Chloride Injection 20 mEq, packaged in 100 mL bags, due to incorrect overwrap labels stating 10 mEq instead of 20 mEq. The recall focuses on lot number 1023172 (NDC 0990-7074-26) with an expiration date of January 31, 2026.
This mislabeling issue was identified during internal review, and the company has halted distribution of the affected product.
The recall applies to shipments provided to healthcare facilities across the United States. The total number of affected units has not been disclosed. ICU Medical is coordinating with regulatory agencies, removing the mislabeled items from circulation, and advising purchasers on returns and refunds.
What to look for?
Product name and description:
- Potassium Chloride Injection 20 mEq, 100 mL bags
- Overwrap labels incorrectly showing Potassium Chloride Injection 10 mEq
- Packaged in cases labeled:
- NDC 0990-7075-26, CASE PACK 124 100ML 20MEQ POTASSIUM CHLORIDE INJECTION LOT NO.1023172, EXP. DATE 2026-01
Identifiers:
- Lot number: 1023172 (NDC 0990-7074-26)
- Expiration date: January 31, 2026
- This information is on the overwrap and box labeling
Affected purchase locations and dates:
- Distributed nationwide to hospitals, clinics, and other medical facilities
- Shipped between January 2023 and August 2023
What should buyers do?
Handling the recalled product:
- Do not use the affected bags
- Return them to the place of purchase or the distributor
Refunds, replacements, or repairs:
- Contact ICU Medical Customer Support at (844) 654-7780 for return instructions and refund or replacement details
- Assistance is available MondayFriday, 9 AM5 PM EST
Health and safety advice:
- Mislabeling may lead to an overdose of potassium, causing possible hyperkalemia
- Symptoms can include muscle weakness, vertigo, confusion, and irregular heartbeat
- Seek immediate medical help if any adverse health effects occur
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AFTCO recalls Youth Solitude Rain Jackets due to strangulation hazard
Check your child's jacket for safety; refunds or gift cards available.
February 14, 2025AFTCO has announced a voluntary recall of its Youth Solitude Rain Jackets (model number BJ05) because the drawstring in the hood can become caught on objects, creating a strangulation hazard. This issue violates federal regulations for children's upper outerwear. The recall affects about 820 units.
No injuries have been reported, and the issue was identified during a compliance review. The jackets were sold nationwide through authorized retailers and online. AFTCO has removed all affected products from circulation and is working with regulatory agencies to resolve the matter. The company is offering refunds or other remedies to those who purchased the recalled jackets.
What to look for?
Product name and description:
- Black Youth Solitude Rain Jacket
- Available in youth sizes XS (5-6), S (6-7), M (8-10), and L (10-12)
- Waterproof nylon design with retractable hood drawstring
- Features the AFTCO logo on the front
Identifiers:
- Model number: BJ05
- The model number is usually printed on the inside label of the jacket
Affected purchase locations and dates:
- Sold through authorized sporting goods retailers and online stores
- If you purchased the jacket recently, check the model number to verify if it is part of the recall
What should buyers do?
Recommended actions:
- Immediately stop children from wearing the jacket
- Remove the hood drawstring to reduce the risk of harm
- Return the jacket directly to AFTCO for a full refund or upload a photo of the jacket without the drawstring to receive a $25 gift card, following instructions provided below
Refunds, replacements, or repairs:
- Contact AFTCO at 877-489-4278 from 7 AM to 3:30 PM PT, Monday through Friday
- Send an email to recall@aftco.com to request a prepaid return label or information on submitting a photo of the drawstring-free jacket
- Additional assistance and recall program details are available on the AFTCO recall participation page
Health and safety advice:
- There are no reported injuries related to the recalled jackets
- If a child has experienced any breathing difficulty or related incidents while wearing the jacket, consider seeking medical evaluation
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Urgent Recall: 6-in-1 Pounding Game from Temu.com poses magnet ingestion risk
Magnet Hazard Alert: Dispose of 6-in-1 Game from Temu.com Now
February 14, 2025A mandated recall has been issued for the 6-in-1 Pounding Game due to a magnet that can come loose and pose an ingestion hazard. The recall was prompted by the U.S. Consumer Product Safety Commissions findings regarding a violation of federal regulations for magnets.
This issue was identified through regulatory oversight, and it affects about 180 units sold exclusively on Temu.com. The company is instructing purchasers to remove the product from use and dispose of it, with instructions for verifying disposal and potentially seeking further assistance.
What to look for?
Product name and description:
- 6-in-1 Pounding Game
- Constructed of wood and includes a frog clock, xylophone, gears, wooden pegs with animal faces, carrots, worms with metal heads, mallets, sticks, and a wooden bird
Identifiers:
- The toy is described as having a magnet embedded in the wooden birds beak
- This embed can break off and create a hazard
- The product packaging may reference 6 in 1
- There is no clearly marked batch or model number on publicly available information
Affected purchase locations and dates:
- Sold exclusively on Temu.com
- No specific date range has been confirmed in public disclosures
What should buyers do?
Next steps:
- Stop using the recalled product
- Keep it away from children
- Dispose of it so it cannot be retrieved by a child
- Take a photo of the disposed product and send it to DMITOY at dmitoy202405@163.com or via message on Temu.com
Refunds, replacements, or repairs:
- Contact DMITOY at dmitoy202405@163.com or through Temu.com for information on refunds or further instructions
Health and safety advice:
- If a magnet was swallowed or there are signs of ingestion, seek immediate medical attention
- Watch for symptoms such as abdominal pain, vomiting, or discomfort
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